دورية أكاديمية

The novel role of circular RNA ST3GAL6 on blocking gastric cancer malignant behaviours through autophagy regulated by the FOXP2/MET/mTOR axis

التفاصيل البيبلوغرافية
العنوان: The novel role of circular RNA ST3GAL6 on blocking gastric cancer malignant behaviours through autophagy regulated by the FOXP2/MET/mTOR axis
المؤلفون: Penghui Xu, Xing Zhang, Jiacheng Cao, Jing Yang, Zetian Chen, Weizhi Wang, Sen Wang, Lu Zhang, Li Xie, Lang Fang, Yiwen Xia, Zhe Xuan, Jialun Lv, Hao Xu, Zekuan Xu
المصدر: Clinical and Translational Medicine, Vol 12, Iss 1, Pp n/a-n/a (2022)
بيانات النشر: Wiley, 2022.
سنة النشر: 2022
المجموعة: LCC:Medicine (General)
مصطلحات موضوعية: autophagy, circST3GAL6, FOXP2, gastric cancer, transcription factor, Medicine (General), R5-920
الوصف: Abstract Gastric cancer (GC) ranks third in mortality among all cancers worldwide. Circular RNAs (circRNAs) play an important role in the occurrence and development of gastric cancer. Forkhead box P2 (FOXP2), as a transcription factor, is closely associated with the development of many types of tumours. However, the regulatory network between FOXP2 and circRNAs remains to be explored. In our study, circST3GAL6 was significantly downregulated in GC and was associated with poor prognosis in GC patients. Overexpression of circST3GAL6 inhibited the malignant behaviours of GC cells, which was mediated by inducing apoptosis and autophagy. In addition, we demonstrated that circST3GAL6 regulated FOXP2 through the mir‐300 sponge. We further found that FOXP2 inhibited MET Proto‐Oncogene (MET), which was the initiating factor that regulated the classic AKT/mTOR pathway of autophagy. In conclusion, our results suggested that circST3GAL6 played a tumour suppressive role in gastric cancer through miR‐300/FOXP2 axis and regulated apoptosis and autophagy through FOXP2‐mediated transcriptional inhibition of the MET axis, which may become a potential target for GC therapy.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2001-1326
Relation: https://doaj.org/toc/2001-1326
DOI: 10.1002/ctm2.707
URL الوصول: https://doaj.org/article/66c440a3a5314769bcfe988c6a0c9ba5
رقم الأكسشن: edsdoj.66c440a3a5314769bcfe988c6a0c9ba5
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20011326
DOI:10.1002/ctm2.707